Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Actr1b |
A |
G |
1: 36,741,168 (GRCm39) |
F138L |
possibly damaging |
Het |
Adamts14 |
G |
T |
10: 61,041,301 (GRCm39) |
P803Q |
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
Akt3 |
A |
G |
1: 176,930,551 (GRCm39) |
S136P |
possibly damaging |
Het |
Aldh16a1 |
C |
T |
7: 44,796,585 (GRCm39) |
|
probably null |
Het |
Alg12 |
A |
G |
15: 88,696,318 (GRCm39) |
W238R |
probably damaging |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,383,888 (GRCm39) |
C1144S |
probably benign |
Het |
Arhgef40 |
G |
A |
14: 52,233,640 (GRCm39) |
V829M |
probably damaging |
Het |
Atg7 |
C |
A |
6: 114,680,324 (GRCm39) |
N344K |
probably damaging |
Het |
Aunip |
T |
A |
4: 134,250,618 (GRCm39) |
S188T |
probably benign |
Het |
Bmpr1b |
A |
T |
3: 141,576,568 (GRCm39) |
H88Q |
probably benign |
Het |
Brpf3 |
G |
A |
17: 29,040,338 (GRCm39) |
G920S |
probably benign |
Het |
Cdc123 |
C |
T |
2: 5,800,354 (GRCm39) |
|
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,817,062 (GRCm39) |
R100G |
probably benign |
Het |
Cdkn2d |
A |
G |
9: 21,202,175 (GRCm39) |
V24A |
probably damaging |
Het |
Cirbp |
T |
C |
10: 80,006,166 (GRCm39) |
|
probably benign |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Col12a1 |
A |
G |
9: 79,569,736 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
A |
15: 8,215,649 (GRCm39) |
S402T |
probably damaging |
Het |
Cpox |
T |
A |
16: 58,494,772 (GRCm39) |
C270S |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,803,940 (GRCm39) |
D1677G |
probably damaging |
Het |
Cyp4a10 |
T |
A |
4: 115,381,917 (GRCm39) |
|
probably benign |
Het |
Dctn4 |
T |
C |
18: 60,671,349 (GRCm39) |
F74L |
possibly damaging |
Het |
Dennd5a |
G |
A |
7: 109,497,900 (GRCm39) |
|
probably benign |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnah9 |
C |
T |
11: 66,036,261 (GRCm39) |
S185N |
probably benign |
Het |
Dqx1 |
T |
G |
6: 83,035,524 (GRCm39) |
|
probably benign |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Ep400 |
A |
C |
5: 110,883,270 (GRCm39) |
|
probably benign |
Het |
Epha1 |
G |
T |
6: 42,342,987 (GRCm39) |
H187Q |
probably benign |
Het |
Fbn2 |
C |
T |
18: 58,181,921 (GRCm39) |
E1827K |
probably damaging |
Het |
Fbxo41 |
C |
T |
6: 85,455,453 (GRCm39) |
W577* |
probably null |
Het |
Fgd6 |
G |
A |
10: 93,880,903 (GRCm39) |
A586T |
probably damaging |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm12888 |
A |
T |
4: 121,182,069 (GRCm39) |
W8R |
unknown |
Het |
Gm2959 |
A |
G |
14: 42,235,658 (GRCm39) |
|
noncoding transcript |
Het |
Gm6214 |
A |
G |
3: 140,544,978 (GRCm39) |
|
noncoding transcript |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gmeb2 |
A |
G |
2: 180,895,763 (GRCm39) |
L469P |
probably benign |
Het |
Gosr1 |
T |
C |
11: 76,628,224 (GRCm39) |
I177V |
probably benign |
Het |
Gria1 |
T |
C |
11: 57,208,534 (GRCm39) |
F810L |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,245,340 (GRCm39) |
Q533* |
probably null |
Het |
Hadhb |
T |
A |
5: 30,378,796 (GRCm39) |
|
probably null |
Het |
Hat1 |
A |
T |
2: 71,240,504 (GRCm39) |
Y66F |
possibly damaging |
Het |
Hk1 |
T |
C |
10: 62,122,315 (GRCm39) |
Y488C |
probably benign |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il19 |
T |
C |
1: 130,866,854 (GRCm39) |
H42R |
probably benign |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Impg2 |
G |
A |
16: 56,063,993 (GRCm39) |
|
probably null |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,636,361 (GRCm39) |
F683S |
probably damaging |
Het |
Itih2 |
A |
G |
2: 10,135,385 (GRCm39) |
S2P |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,317,050 (GRCm39) |
M768I |
probably benign |
Het |
Kcnab1 |
A |
G |
3: 65,272,060 (GRCm39) |
E315G |
probably benign |
Het |
Kcnmb2 |
A |
C |
3: 32,252,437 (GRCm39) |
I213L |
probably damaging |
Het |
Khdc1a |
T |
A |
1: 21,421,196 (GRCm39) |
M127K |
probably benign |
Het |
Klhl28 |
T |
C |
12: 64,990,246 (GRCm39) |
N565S |
probably benign |
Het |
Lcp1 |
A |
G |
14: 75,435,515 (GRCm39) |
|
probably null |
Het |
Mcm4 |
T |
C |
16: 15,452,333 (GRCm39) |
T267A |
possibly damaging |
Het |
Mlxipl |
A |
T |
5: 135,161,631 (GRCm39) |
T517S |
possibly damaging |
Het |
Mpp3 |
T |
A |
11: 101,891,516 (GRCm39) |
I541L |
probably benign |
Het |
Mpp4 |
G |
A |
1: 59,182,941 (GRCm39) |
P322L |
possibly damaging |
Het |
Myh15 |
G |
A |
16: 48,975,984 (GRCm39) |
A1351T |
possibly damaging |
Het |
Nacc1 |
A |
T |
8: 85,399,747 (GRCm39) |
M490K |
probably benign |
Het |
Nbeal1 |
C |
A |
1: 60,309,515 (GRCm39) |
Q496K |
possibly damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or14j1 |
T |
A |
17: 38,145,893 (GRCm39) |
M1K |
probably null |
Het |
Pard3 |
T |
C |
8: 128,337,092 (GRCm39) |
L1236P |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Phf21a |
C |
A |
2: 92,157,422 (GRCm39) |
N183K |
possibly damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Prl3c1 |
G |
A |
13: 27,380,720 (GRCm39) |
|
probably null |
Het |
Prl7a2 |
T |
A |
13: 27,844,870 (GRCm39) |
Y172F |
probably damaging |
Het |
Psg16 |
T |
G |
7: 16,827,673 (GRCm39) |
S210A |
possibly damaging |
Het |
Psg25 |
T |
A |
7: 18,255,178 (GRCm39) |
K446M |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,050,388 (GRCm39) |
|
probably benign |
Het |
Rgs7 |
A |
T |
1: 174,949,508 (GRCm39) |
F160L |
probably damaging |
Het |
Rpl22l1 |
A |
T |
3: 28,860,957 (GRCm39) |
E57D |
possibly damaging |
Het |
Rpl35 |
A |
G |
2: 38,894,753 (GRCm39) |
L44P |
possibly damaging |
Het |
Rtn4r |
T |
C |
16: 17,969,121 (GRCm39) |
L183P |
probably damaging |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Slc4a7 |
G |
A |
14: 14,733,773 (GRCm38) |
R67H |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,756,090 (GRCm39) |
|
probably benign |
Het |
Smurf2 |
T |
C |
11: 106,762,374 (GRCm39) |
T39A |
probably damaging |
Het |
Sspo |
A |
T |
6: 48,450,596 (GRCm39) |
D2595V |
probably damaging |
Het |
Tatdn2 |
A |
G |
6: 113,681,103 (GRCm39) |
K379E |
probably benign |
Het |
Tbc1d14 |
G |
A |
5: 36,680,274 (GRCm39) |
R68* |
probably null |
Het |
Tgm1 |
A |
G |
14: 55,946,928 (GRCm39) |
I360T |
probably damaging |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Traf1 |
A |
T |
2: 34,838,202 (GRCm39) |
I212N |
probably benign |
Het |
Ttc17 |
C |
A |
2: 94,196,892 (GRCm39) |
W485L |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,768,675 (GRCm39) |
V2920F |
probably damaging |
Het |
Tyr |
T |
C |
7: 87,142,051 (GRCm39) |
I93V |
probably benign |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Vmn1r212 |
A |
G |
13: 23,068,285 (GRCm39) |
V16A |
probably benign |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,553 (GRCm39) |
H412L |
possibly damaging |
Het |
Xirp1 |
T |
C |
9: 119,845,962 (GRCm39) |
I974V |
probably benign |
Het |
Zap70 |
A |
G |
1: 36,818,215 (GRCm39) |
T301A |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,463,987 (GRCm39) |
K1382E |
probably damaging |
Het |
Zfp280b |
T |
A |
10: 75,875,017 (GRCm39) |
C299S |
probably damaging |
Het |
Zfp352 |
C |
T |
4: 90,113,357 (GRCm39) |
S499L |
probably benign |
Het |
Zfp423 |
G |
A |
8: 88,507,986 (GRCm39) |
A661V |
probably benign |
Het |
Zfp57 |
T |
A |
17: 37,320,568 (GRCm39) |
F141I |
possibly damaging |
Het |
Zfp946 |
A |
T |
17: 22,674,446 (GRCm39) |
H400L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Exoc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00095:Exoc2
|
APN |
13 |
31,004,609 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01839:Exoc2
|
APN |
13 |
31,090,782 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Exoc2
|
APN |
13 |
31,059,260 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02245:Exoc2
|
APN |
13 |
31,090,842 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02267:Exoc2
|
APN |
13 |
30,999,304 (GRCm39) |
missense |
probably benign |
|
IGL02478:Exoc2
|
APN |
13 |
31,111,403 (GRCm39) |
missense |
probably benign |
|
IGL02500:Exoc2
|
APN |
13 |
31,095,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03081:Exoc2
|
APN |
13 |
31,084,885 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03112:Exoc2
|
APN |
13 |
31,090,570 (GRCm39) |
splice site |
probably benign |
|
IGL03409:Exoc2
|
APN |
13 |
31,124,720 (GRCm39) |
utr 5 prime |
probably benign |
|
R0284:Exoc2
|
UTSW |
13 |
31,061,608 (GRCm39) |
splice site |
probably benign |
|
R0452:Exoc2
|
UTSW |
13 |
31,070,310 (GRCm39) |
splice site |
probably benign |
|
R0826:Exoc2
|
UTSW |
13 |
31,040,780 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1251:Exoc2
|
UTSW |
13 |
31,070,259 (GRCm39) |
missense |
probably benign |
0.03 |
R1367:Exoc2
|
UTSW |
13 |
31,066,256 (GRCm39) |
nonsense |
probably null |
|
R1501:Exoc2
|
UTSW |
13 |
31,119,485 (GRCm39) |
missense |
probably benign |
0.01 |
R1593:Exoc2
|
UTSW |
13 |
31,040,744 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1839:Exoc2
|
UTSW |
13 |
31,090,480 (GRCm39) |
splice site |
probably benign |
|
R1872:Exoc2
|
UTSW |
13 |
31,006,644 (GRCm39) |
missense |
probably benign |
0.17 |
R2070:Exoc2
|
UTSW |
13 |
30,999,353 (GRCm39) |
missense |
probably benign |
0.00 |
R2227:Exoc2
|
UTSW |
13 |
31,048,867 (GRCm39) |
missense |
probably benign |
|
R2507:Exoc2
|
UTSW |
13 |
31,066,348 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3965:Exoc2
|
UTSW |
13 |
31,061,565 (GRCm39) |
missense |
probably benign |
0.00 |
R4601:Exoc2
|
UTSW |
13 |
31,066,251 (GRCm39) |
missense |
probably benign |
0.05 |
R4914:Exoc2
|
UTSW |
13 |
31,060,796 (GRCm39) |
missense |
probably benign |
0.21 |
R5299:Exoc2
|
UTSW |
13 |
31,055,901 (GRCm39) |
splice site |
probably null |
|
R5410:Exoc2
|
UTSW |
13 |
31,048,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R5461:Exoc2
|
UTSW |
13 |
31,109,738 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5956:Exoc2
|
UTSW |
13 |
31,004,606 (GRCm39) |
missense |
probably benign |
0.03 |
R6056:Exoc2
|
UTSW |
13 |
31,084,812 (GRCm39) |
missense |
probably benign |
0.03 |
R6107:Exoc2
|
UTSW |
13 |
31,060,780 (GRCm39) |
missense |
probably benign |
|
R6548:Exoc2
|
UTSW |
13 |
31,010,047 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6692:Exoc2
|
UTSW |
13 |
31,119,490 (GRCm39) |
missense |
probably benign |
0.09 |
R6969:Exoc2
|
UTSW |
13 |
31,095,161 (GRCm39) |
missense |
probably benign |
|
R7386:Exoc2
|
UTSW |
13 |
31,090,646 (GRCm39) |
splice site |
probably null |
|
R7461:Exoc2
|
UTSW |
13 |
31,066,255 (GRCm39) |
missense |
probably benign |
0.32 |
R7467:Exoc2
|
UTSW |
13 |
31,109,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R7473:Exoc2
|
UTSW |
13 |
31,006,613 (GRCm39) |
critical splice donor site |
probably null |
|
R7613:Exoc2
|
UTSW |
13 |
31,066,255 (GRCm39) |
missense |
probably benign |
0.32 |
R7767:Exoc2
|
UTSW |
13 |
31,060,752 (GRCm39) |
missense |
probably benign |
0.01 |
R7793:Exoc2
|
UTSW |
13 |
31,095,161 (GRCm39) |
missense |
probably benign |
0.00 |
R7795:Exoc2
|
UTSW |
13 |
31,060,756 (GRCm39) |
nonsense |
probably null |
|
R7993:Exoc2
|
UTSW |
13 |
31,090,713 (GRCm39) |
critical splice donor site |
probably null |
|
R8085:Exoc2
|
UTSW |
13 |
31,124,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R8330:Exoc2
|
UTSW |
13 |
31,061,556 (GRCm39) |
missense |
probably benign |
|
R8716:Exoc2
|
UTSW |
13 |
31,095,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Exoc2
|
UTSW |
13 |
31,090,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Exoc2
|
UTSW |
13 |
31,055,838 (GRCm39) |
missense |
probably benign |
0.05 |
R9237:Exoc2
|
UTSW |
13 |
31,048,858 (GRCm39) |
missense |
probably benign |
|
R9243:Exoc2
|
UTSW |
13 |
31,109,778 (GRCm39) |
missense |
probably benign |
0.03 |
R9365:Exoc2
|
UTSW |
13 |
31,040,697 (GRCm39) |
missense |
probably benign |
0.00 |
R9731:Exoc2
|
UTSW |
13 |
31,061,233 (GRCm39) |
missense |
probably benign |
0.06 |
|